The Mammalian Reproductive Genetics DatabaseCurrent FeaturesThe Mammalian Reproductive Genetics website (MRG) is a research community resource designed to collectand disseminate information regarding genes involved in mammalian reproduction. In addition, it is hoped thatthe MRG will increase the interactions between members of the research community, through use of adiscussion forum and mailing list, which can be used to discuss topics of general and specific interest.The MRG contains the transcription expression profile of several different cell types and tissues. Thelaboratory of Dr. Mike Griswold has provided data from experiments using microarray analysis of thetranscription profiles of the male and female mouse embryos at embryonic day 11.5, 12.5, 14.5, 16.5, and18.5, the mouse testis at postnatal day 0, 3, 6, 8,10, 14, 18, 20, 30, 35, and 56, and different cell types fromadult testis. These cell types include myoid cells and Sertoli cells from 16-18 day old animals, and type A andB spermatogonia, pachytene spermatocytes, and round spermatids from animals 8, 30, and 60 days of age,respectively. The expression profiles of individual genes can be accessed by searching for gene name, genesymbol, Mouse Genome Informatics number, or Affymetrix probe number.The MRG also contains phenotypic data. These data are added to the database by individual researchers orare curated by MRG staff. Each instance of phenotype data is associated with an article published in a peerreviewedjournal, and so provenance is established.Information regarding individual genes can be searched for by gene name or symbol, Mouse GenomeInformatics number, or Affymetrix probe set id number. In addition, the text of the submissions that have beenentered into the MRG can be searched. The results of the search can contain both expression and phenotypedata, if such data is contained in the MRG databases. Additionally, the search results will include links to othersites with information on the gene. These sites include Jackson Labs, SwissProt, NCBI's Unigene and LocusLink, GermOnline, and Genbank.As well as searching for information on individual genes, it is possible to search for all genes identified as beingexpressed in tissues or cell types for which we have data, or mutation of which results in a particularphenotype. Information on the genes in the list returned by such a search can then themselves be obtained.For example, one can search for genes associated with infertility and then search for those genes on the MRG,to see at what developmental time point, in what tissues and at what levels those genes are expressed.In addition to providing scientific researchers with a resource for accessing information regarding genesinvolved in reproduction, we hope that the MRG can be used to increase the sense of community amongindividuals and groups. To that end we have included on the MRG a mailing list and a discussion forum. Themailing list allows email messages to be sent to all who choose to subscribe to it. The discussion forum allowsresearchers to interact by posting messages and replies which are held on the MRG.The MRG has some helpful tools for scientists engaged in reproductive biology research. There is thePubmed Autosearch, which automatically searches Pubmed for article abstracts and keywords for user definedtext. The search frequency is user defined, and the results of the search are returned in an email. There arealso a variety of links to useful websites, including links to reproductive biology journals, sites of interest, suchas the Reproductive Genomics Program at the Jackson Labs and GermOnline. Researchers are alsoencouraged to submit links to their lab web pages.Future FeaturesWe continue to add expression and phenotype data to the MRG. In the near term future, we will be addingtranscription expression profiles of epididymal segments. This data is to be provided by Wyeth (see letter ofsupport). We also encourage other researchers to deposit expression data at the MRG, and will activelypursue published datasets.There are also a number of features, that could be added to the MRG to improve the usefulness of the site.Some researchers have indicated that it would be helpful to be able to search the MRG databases usingontological keyword searches. This would allow, for example, the search for all tyrosine kinases expressed inSertoli cells. Implementing this type of search would require deciding on an ontological schema. Rather thandeveloping our own, we would likely use the schema developed by the Mouse Genome Informatics group atthe Jackson Labs.Many researchers could be aided by the illustrated presentation of a spermatogenic staging. This wouldinclude images of the different stages of spermatogenesis, using testis sections with different fixation methodsand different histolbgical stains. In a similar vein, the presentation of neuroendocrine hormone pathwaysinvolved in spermatogenesis and oogenesis would be a valuable tool for the research community. The proteinnames in the pathway could be active links leading to expression and phenotypic data contained within theMRG. Some of the pathways to be elucidated would include the pituitary-gonadal axis and the androgensynthesis pathway.A valuable resource for the reproductive community would be the establishment of a database of cell typemarkers. This could include antibodies and associated proteins, which would require the involvement ofadditional laboratories. The MRG staff could take responsibility for collecting and curating the marker list, thusincreasing the likelihood of participation. We could also allow researchers the opportunity to comment on theusefulness of the markers listed. Another possible model is for members of the research community to submitmarker data.Meeting reviews are another area where the MRG may contribute to the research community. We couldcollaborate with journal editors to arrange for meeting attendees to write a meeting review, which would bepublished both in print and on the MRG. Alternatively, MRG staff could solicit authors independently and editand publish the content.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Specialized Center--Cooperative Agreements (U54)
Project #
5U54HD012629-29
Application #
7722611
Study Section
Special Emphasis Panel (ZHD1-DRG-D (04))
Project Start
2008-04-01
Project End
2011-03-31
Budget Start
2008-04-01
Budget End
2009-03-31
Support Year
29
Fiscal Year
2008
Total Cost
$214,667
Indirect Cost
Name
University of Washington
Department
Type
DUNS #
605799469
City
Seattle
State
WA
Country
United States
Zip Code
98195
Chakraborty, Papia; Buaas, F William; Sharma, Manju et al. (2014) LIN28A marks the spermatogonial progenitor population and regulates its cyclic expansion. Stem Cells 32:860-73
Sanz, Elisenda; Evanoff, Ryan; Quintana, Albert et al. (2013) RiboTag analysis of actively translated mRNAs in Sertoli and Leydig cells in vivo. PLoS One 8:e66179
Cazorla, Maxime; Shegda, Mariya; Ramesh, Bhavani et al. (2012) Striatal D2 receptors regulate dendritic morphology of medium spiny neurons via Kir2 channels. J Neurosci 32:2398-409
Gill, John C; Navarro, VĂ­ctor M; Kwong, Cecilia et al. (2012) Increased neurokinin B (Tac2) expression in the mouse arcuate nucleus is an early marker of pubertal onset with differential sensitivity to sex steroid-negative feedback than Kiss1. Endocrinology 153:4883-93
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Navarro, Victor M; Ruiz-Pino, Francisco; Sanchez-Garrido, Miguel A et al. (2012) Role of neurokinin B in the control of female puberty and its modulation by metabolic status. J Neurosci 32:2388-97
Roth, M Y; Page, S T; Lin, K et al. (2011) The effect of gonadotropin withdrawal and stimulation with human chorionic gonadotropin on intratesticular androstenedione and DHEA in normal men. J Clin Endocrinol Metab 96:1175-81
Roth, M Y; Amory, J K (2011) Pharmacologic development of male hormonal contraceptive agents. Clin Pharmacol Ther 89:133-6
Navarro, V M; Gottsch, M L; Wu, M et al. (2011) Regulation of NKB pathways and their roles in the control of Kiss1 neurons in the arcuate nucleus of the male mouse. Endocrinology 152:4265-75
Navarro, Victor M; Castellano, Juan M; McConkey, Sarah M et al. (2011) Interactions between kisspeptin and neurokinin B in the control of GnRH secretion in the female rat. Am J Physiol Endocrinol Metab 300:E202-10

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